Elevated levels of PAI-1 activity and t-PA antigen are associated with newly diagnosed abnormal glucose regulation in patients with ST-elevation myocardial infarction

J Thromb Haemost. 2011 Aug;9(8):1468-74. doi: 10.1111/j.1538-7836.2011.04377.x.

Abstract

Background: Both Type 2 diabetes and cardiovascular disease have been associated with enhanced coagulation and suppressed fibrinolysis.

Objectives: To investigate a possible relationship between selected hemostatic variables and abnormal glucose regulation (AGR) in patients with acute ST-elevation myocardial infarction (STEMI) without known diabetes and to study changes in selected hemostatic variables from baseline to follow-up in STEMI patients with or without AGR.

Methods: Plasminogen activator inhibitor-1 (PAI-1) activity, tissue plasminogen activator (t-PA) antigen, prothrombin fragment 1+2 (F(1+2)) and von Willebrand factor (vWF) were measured in fasting blood samples from 199 STEMI patients 16.5 h (median time) after admission and 3 months later. All patients were classified into normal glucose regulation (NGR) or AGR based on an oral glucose tolerance test at follow-up, according to the WHO criteria.

Results: High PAI-1 activity (≥ 75th percentile) measured in-hospital was associated with AGR (n = 49) with an adjusted odds ratio of 2.2 (95% confidence interval, 1.1, 4.4). In addition, high levels of t-PA antigen (≥ 75th percentile) were associated with AGR (adjusted odds ratio, 3.5; 95% confidence inteval, 1.5, 8.2), but only in men. Changes in the levels of F(1+2) were significantly more pronounced in patients with AGR compared with NGR (adjusted P = 0.04).

Conclusion: Elevated levels of PAI-1 activity and t-PA antigen measured in-hospital in STEMI patients were associated with AGR classified at 3-month follow-up. Additionally, changes in the levels of F(1+2) were more pronounced in patients with AGR compared with NGR. The data suggest an enhanced prothrombotic state after an acute STEMI in patients with AGR without known diabetes.

Trial registration: ClinicalTrials.gov NCT00926133.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Biomarkers / blood
  • Blood Glucose / metabolism*
  • Chi-Square Distribution
  • Diabetes Mellitus, Type 2 / blood*
  • Diabetes Mellitus, Type 2 / diagnosis
  • Female
  • Glucose Intolerance / blood*
  • Glucose Intolerance / diagnosis
  • Glucose Tolerance Test
  • Hemostasis*
  • Humans
  • Inpatients
  • Logistic Models
  • Male
  • Myocardial Infarction / blood*
  • Myocardial Infarction / diagnosis
  • Norway
  • Odds Ratio
  • Peptide Fragments / blood
  • Plasminogen Activator Inhibitor 1 / blood*
  • Prospective Studies
  • Prothrombin
  • Time Factors
  • Tissue Plasminogen Activator / blood*
  • Up-Regulation
  • von Willebrand Factor / metabolism

Substances

  • Biomarkers
  • Blood Glucose
  • Peptide Fragments
  • Plasminogen Activator Inhibitor 1
  • SERPINE1 protein, human
  • prothrombin fragment 1.2
  • von Willebrand Factor
  • Prothrombin
  • Tissue Plasminogen Activator

Associated data

  • ClinicalTrials.gov/NCT00926133